Showing results (681-690 of 796) with videos related to
Sort By:
Pageof 80
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.European Heart Journal|December 22, 2020
Effect of empagliflozin on exercise ability and symptoms in heart failure patients with reduced and preserved ejection fraction, with and without type 2 diabetesWilliam T Abraham, JoAnn Lindenfeld, Piotr Ponikowski, et al.American Journal of Human Genetics|August 16, 2016
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in InfancyAnne Guimier, Christopher T Gordon, François Godard, et al.Blood Pressure|November 2, 2018
2018 Practice Guidelines for the management of arterial hypertension of the European Society of Cardiology and the European Society of HypertensionBryan Williams, Giuseppe Mancia, Wilko Spiering, et al.Genome Research|November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genomeHeike Fiegler, Richard Redon, Dan Andrews, et al.BMC Psychiatry|July 3, 2024
Adherence to clinical practice guidelines for using electroconvulsive therapy in elderly depressive patientsAntoine Yrondi, Olivier Blanc, Loic Anguill, et al.Nature Communications|January 26, 2018
Parallel derivation of isogenic human primed and naive induced pluripotent stem cellsStéphanie Kilens, Dimitri Meistermann, Diego Moreno, et al.Physical Review Letters|December 31, 2005
Excitation energies of superdeformed States in 196Pb: towards a systematic study of the second well in Pb isotopesA N Wilson, A K Singh, H Hübel, et al.Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.Neurology|October 15, 2021
Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic StudyFlorence Riant, Caroline Roos, Agathe Roubertie, et al.Pageof 80